Experimental Factor Ontology
6962 terms(s) returned
| Term Type: | Record: 5151 to 5200 of 6962 Records | Page: 104 of 140, First Previous Next Last | Show Records Per Page |
- programmed cell death protein 1 measurement
- programmed cell death protein 1, signal peptide removed form (human)
- programmed cell death protein 4
- programmed cell death protein 4 (human)
- programmed cell death protein 5
- programmed cell death protein 5 (human)
- programmed cell death protein 5 measurement
- programmed cell death protein 5, initiator methionine removed form
- programmed cell death protein 6
- programmed cell death protein 6 (human)
- programmed death-ligand 1 measurement
- progranulin
- progranulin (human)
- progranulin measurement
- progranulin proteolytic cleavage product
- progranulin, signal peptide removed form
- progranulin, signal peptide removed form (human)
- progression free survival
- progressive bifocal chorioretinal atrophy
- progressive bulbar palsy
- progressive bulbar palsy of childhood
- progressive cavitating leukoencephalopathy
- progressive cerebello-cerebral atrophy
- progressive deafness with stapes fixation
- progressive demyelinating neuropathy with bilateral striatal necrosis
- progressive encephalopathy with leukodystrophy due to DECR deficiency
- progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome
- progressive external ophthalmoplegia
- progressive external ophthalmoplegia with mitochondrial DNA deletions
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5
- progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6
- progressive familial heart block
- progressive familial heart block, type 1A
- progressive familial intrahepatic cholestasis
- progressive familial intrahepatic cholestasis type 1
- progressive familial intrahepatic cholestasis type 2
- progressive familial intrahepatic cholestasis type 3
- progressive microcephaly-seizures-cortical blindness-developmental delay syndrome
- progressive multifocal leukoencephalopathy
- progressive muscular dystrophy
- progressive myoclonic epilepsy type 3
